Canonical Allele Identifier: CA1173064335

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259051T= , CM000663.2:g.67259051T=	GRCh38
NC_000001.10:g.67724734T= , CM000663.1:g.67724734T=	GRCh37
NC_000001.9:g.67497322T=	NCBI36
NG_011498.1:g.97566T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1652T=	ENSP00000513138.1:n.1652T=
ENST00000697150.1:c.1710T=	ENSP00000513139.1:n.1710T=
ENST00000697151.1:c.1643T=	ENSP00000513140.1:n.1643T=
ENST00000697164.1:c.1723T=	ENSP00000513153.1:p.Leu575=
ENST00000697165.1:c.1510T=	ENSP00000513154.1:p.Leu504=
ENST00000347310.10:c.1813T= MANE Select	ENSP00000321345.5:p.Leu605=
ENST00000637002.1:c.1204T=	ENSP00000490340.1:p.Leu402=
ENST00000347310.9:c.1813T=	ENSP00000321345.5:p.Leu605=
ENST00000395227.2:c.607T=	ENSP00000378652.2:p.Leu203=
ENST00000425614.3:c.1048T=	ENSP00000387640.2:p.Leu350=
ENST00000473881.2:c.*639T=	ENSP00000486667.1:n.*639T=
NM_144701.2:c.1813T=	NP_653302.2:p.Leu605=
XM_005270516.2:c.1051T=	XP_005270573.1:p.Leu351=
XM_011540789.1:c.1903T=	XP_011539091.1:p.Leu635=
XM_011540790.1:c.1813T=	XP_011539092.1:p.Leu605=
XM_011540791.1:c.1813T=	XP_011539093.1:p.Leu605=
XM_011540790.3:c.1813T=	XP_011539092.1:p.Leu605=
XM_011540791.3:c.1813T=	XP_011539093.1:p.Leu605=
XR_001736993.1:n.1893T=
NM_144701.3:c.1813T= MANE Select	NP_653302.2:p.Leu605=